Metformin Hydrochloride
- Product NDC
- 70518-3212
- 11-digit product format
- 705183212
- Labeler code
- 70518
- Product ID
- 70518-3212_ea3a8b8a-37ec-37c1-e053-2a95a90acc91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205096
- Marketing category
- ANDA
- Marketing start
- 2021-09-03
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3212-0 | 70518321200 | 30 TABLET, COATED in 1 BLISTER PACK (70518-3212-0) | 2021-09-03 | 0000-00-00 | No | No | Current |
| 70518-3212-1 | 70518321201 | 180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3212-1) | 2022-07-06 | 0000-00-00 | No | No | Current |
| 70518-3212-2 | 70518321202 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3212-2) | 2022-07-17 | 0000-00-00 | No | No | Current |